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Development of a modular, biocompatible thiolated gelatin microparticle platform for drug delivery and tissue engineering applications
被引:10
|作者:
Pearce, Hannah A.
[1
]
Kim, Yu Seon
[1
]
Watson, Emma
[1
]
Bahrami, Kiana
[1
]
Smoak, Mollie M.
[1
]
Jiang, Emily Y.
[1
]
Elder, Michael
[1
]
Shannon, Tate
[1
]
Mikos, Antonios G.
[1
]
机构:
[1] Rice Univ, Dept Bioengn, 6500 Main St, Houston, TX 77030 USA
基金:
美国国家卫生研究院;
美国国家科学基金会;
关键词:
gelatin microparticles;
thiolated gelatin microparticles;
click chemistry;
cell delivery;
drug delivery;
tissue engineering;
biomaterials;
MESENCHYMAL STEM-CELLS;
BIODEGRADABLE HYDROGEL COMPOSITES;
CALCIUM-PHOSPHATE CEMENT;
GROWTH-FACTOR DELIVERY;
TRANSFORMING GROWTH-FACTOR-BETA-1;
PHYSICOCHEMICAL CHARACTERIZATION;
CHONDROGENIC DIFFERENTIATION;
RELEASE KINETICS;
CLICK REACTIONS;
FUNCTIONALIZATION;
D O I:
10.1093/rb/rbab012
中图分类号:
TB3 [工程材料学];
R318.08 [生物材料学];
学科分类号:
0805 ;
080501 ;
080502 ;
摘要:
The field of biomaterials has advanced significantly in the past decade. With the growing need for high-throughput manufacturing and screening, the need for modular materials that enable streamlined fabrication and analysis of tissue engineering and drug delivery schema has emerged. Microparticles are a powerful platform that have demonstrated promise in enabling these technologies without the need to modify a bulk scaffold. This building block paradigm of using microparticles within larger scaffolds to control cell ratios, growth factors and drug release holds promise. Gelatin microparticles (GMPs) are a well-established platform for cell, drug and growth factor delivery. One of the challenges in using GMPs though is the limited ability to modify the gelatin post-fabrication. In the present work, we hypothesized that by thiolating gelatin before microparticle formation, a versatile platform would be created that preserves the cytocompatibility of gelatin, while enabling post-fabrication modification. The thiols were not found to significantly impact the physicochemical properties of the microparticles. Moreover, the thiolated GMPs were demonstrated to be a biocompatible and robust platform for mesenchymal stem cell attachment. Additionally, the thiolated particles were able to be covalently modified with a maleimide-bearing fluorescent dye and a peptide, demonstrating their promise as a modular platform for tissue engineering and drug delivery applications.
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页数:12
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